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논문 기본 정보

자료유형
학술저널
저자정보
Choi Young Im (Biotechnology Division, Korea Forest Research Institute) Noh Eun Woon (Biotechnology Division, Korea Forest Research Institute) Lee Hyo Shin (Biotechnology Division, Korea Forest Research Institute) Han Mu Seok (Biotechnology Division, Korea Forest Research Institute) Lee Jae Soon (Biotechnology Division, Korea Forest Research Institute) Choi Kwan Sam (Department of Applied Science, Chungnam National University)
저널정보
한국식물학회 식물학회지 식물학회지 제48권 제4호
발행연도
2005.1
수록면
351 - 355 (5page)

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A selectable marker gene facilitates the detection of genetically modified plant cells during transformation experiments. So far, these marker genes are almost exclusively of two types, conferring either antibiotic resistance or herbicide tolerance. However, more selectable markers must be developed as additional transgenic traits continue to be incorporated into transgenic plants. Here, we used mercury resistance, conferred by the organomercurial lyase gene, as a selectable marker for transformation. The merB gene from Streptococcus aureus was modified for plant expression and transferred to a hybrid poplar (Populus alba$\times$Populus glandulosa), using the stem segment-agrobacteria cocultivatiion method. The transformed cells were selected on a callus-inducing medium containing as little as $1 {\mu}M$ methylmercury. Subsequent plant regeneration was done in the presence of methylmercury. Resistance to Hg was stably maintained in mature plants after two years of growth in the nursery. We suggest that this gene could serve as an excellent selectable marker for plant transformation.

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